Messages That Motivate: Communicating Alcohol-Related Breast Cancer Risk to Young Adult Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-25
SponsorOhio State University Comprehensive Cancer Center

About this trial

This is an online cross-sectional experimental survey study examining two cancer communication questions: 1) What features of social media messages communicating the breast cancer risks from alcohol consumption will motivate young adult women to drink less? and 2) Do message features differ in their persuasive effects based on young adult women's alcohol consumption behavior?

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Assigned female at birth

Age 18-25

Report drinking alcohol at least once in the past 30 days

Registered in the United States as a member of the Prolific consumer research platform

Disqualifiers

Assigned male at birth

Ages <18 or >25

Do not report drinking alcohol at least once in the past 30 days

Not registered in the U.S. as a member of the Prolific consumer research platform

Trial design

Design model

Parallel

Treatments tested in this trial

  • Risk Message

    Behavioral

    Risk message content

  • Efficacy Message

    Behavioral

    Efficacy Message Content

  • Industry Deception

    Behavioral

    Messages with information about alcohol industry deception

  • YAW Susceptibility

    Behavioral

    Message content with information about why young adult women are susceptible to breast cancer risk from alcohol consumption

  • Mechanisms

    Behavioral

    Message content with information about the mechanism by which alcohol contributes to increased breast cancer risk

Treatment groups

900 Participants
are divided into 9 treatment groups

9

Treatment groups

See each treatment group below.

Group A: Arm 1: Risk Only + Industry DeceptionExperimental treatment 2 interventions
Group B: Arm 2: Risk Only + YAW SusceptibilityExperimental treatment 2 interventions
Group C: Arm 3: Risk Only + MechanismsExperimental treatment 2 interventions
Group D: Arm 4: Efficacy Only + Industry DeceptionExperimental treatment 2 interventions
Group E: Arm 5: Efficacy Only + YAW SusceptibilityExperimental treatment 2 interventions
Group F: Arm 6: Efficacy Only + MechanismsExperimental treatment 2 interventions
Group G: Arm 7: Risk and Efficacy + Industry DeceptionExperimental treatment 3 interventions
Group H: Arm 8: Risk and Efficacy + YAW SusceptibilityExperimental treatment 3 interventions
Group I: Arm 9: Risk and Efficacy + MechanismsExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Message Perceptions

We will assess message perceptions using a valid, reliable measure with six questions about whether participants thought the messages were worth remembering, grabbed their attention, and were informative, powerful, convincing, and meaningful. Responses are on a five-point Likert scale from 1 (Strongly disagree) to 5 (Strongly agree). For all message response outcomes, we will sum and average responses to the items to create message-level scores, then compute means across both messages within each condition for a grand mean. Higher values are considered a better outcome.

Time frame
This assessment is administered immediately after participants view study messages on Day 1
2

Effect Perceptions

We will capture message effects perceptions using the abbreviated effects perceptions scale. Items include questions about how much the messages made them feel discouraged to drink alcohol, concerned about drinking alcohol, and made them feel that drinking alcohol is unpleasant on a scale from 1 (Strongly disagree) to 5 (Strongly agree). For all message response outcomes, we will sum and average responses to the items to create message-level scores, then compute means across both messages within each condition for a grand mean. Higher values are considered a better outcome.

Time frame
This assessment is administered immediately after participants view study messages on Day 1
3

Emotional Response

We will capture emotional responses to the messages using a valid, four item scale. Items are "This message made me angry; irritated; aggravated; and annoyed" with responses on a 5-point Likert scale from 1 (Not likely at all) to 5 (Extremely likely). For all message response outcomes, we will sum and average responses to the items to create message-level scores, then compute means across both messages within each condition for a grand mean. Higher values are considered a better outcome.

Time frame
This assessment is administered immediately after participants view study messages on Day 1
4

Counter-arguing

We will capture counter-arguing, a measure of whether participants cognitively refute messages, with a valid, three item scale that captures whether participants criticize messages, think of points that go against messages, and are skeptical of the messages. Responses are on a 5-point Likert scale ranging from 1 (Not at all) to 7 (Very much). For all message response outcomes, we will sum and average responses to the items to create message-level scores, then compute means across both messages within each condition for a grand mean. Lower values are considered a better outcome.

Time frame
This assessment is administered immediately after participants view study messages on Day 1

Secondary outcomes

Other outcomes

Sponsors and contacts

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Ohio State University Comprehensive Cancer Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: